Mutations in NRXN1 in a family multiply affected with brain disorders: NRXN1 mutations and brain disorders. [electronic resource]
Producer: 20121005Description: 354-8 p. digitalISSN:- 1552-485X
- Adult
- Aged
- Base Sequence
- Brain Diseases -- genetics
- Calcium-Binding Proteins
- Cell Adhesion Molecules, Neuronal -- genetics
- Child
- Child, Preschool
- DNA Mutational Analysis
- Exons -- genetics
- Family
- Female
- Genetic Predisposition to Disease
- Humans
- Infant
- Infant, Newborn
- Introns -- genetics
- Male
- Molecular Sequence Data
- Mutation -- genetics
- Nerve Tissue Proteins -- genetics
- Neural Cell Adhesion Molecules
- Pedigree
- Phenotype
No physical items for this record
Publication Type: Case Reports; Journal Article; Research Support, Non-U.S. Gov't
There are no comments on this title.
Log in to your account to post a comment.